Results 11 to 20 of about 1,226,922 (193)
Journal of Indian Academy of Oral Medicine and Radiology, 2010 Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant inherited disorder characterized by numerous basal cell carcinomas, odontogenic keratocysts, and musculoskeletal malformation. It is occasionally associated
M K Sunil +3 more
doaj +6 more sources
Dental Research Journal, 2012 Gorlin-Goltz syndrome is an uncommon autosomal dominant inherited disorder, which is characterized by multiple odontogenic Keratocysts and basal cell carcinomas, skeletal, dental, ophthalmic, and neurological abnormalities, intracranial ectopic ...
Priya Shirish Joshi +2 more
doaj +8 more sources
Journal of Indian Academy of Oral Medicine and Radiology, 2011 Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent multisystemic disease inherited in a dominant autosomal way, which shows a high level of penetrance and variable expressiveness.
B V Shobha +5 more
doaj +3 more sources
A Case of Male Goltz Syndrome [PDF]
Case Reports in Pediatrics, 2012 We present the case of a boy with a clinical diagnosis of Goltz syndrome (focal dermal hypoplasia), a rare genodermatosis characterized by widespread dysplasia of mesodermal and ectodermal tissues.
Bhaswati Ghoshal +2 more
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Clinical Case ReportsWe report the first female case of Goltz–Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. This case expands the known phenotypic and genotypic spectrum of FDH.
Anna Bolzon +5 more
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Gorlin-Goltz Syndrome with Multiple OKC in a 10-Year-Old Child: A Case Report [PDF]
Journal of Multidisciplinary Dental ResearchGorlin-Goltz syndrome is rare multi-system disease, which is, characterized by neoplasms and other developmental abnormalities. 1 It is a hereditary condition inherited as an autosomal dominant trait and caused by abnormalities in the PTCH1 ...
Devadhakshayani Venkatesan +3 more
doaj +2 more sources
An Unexpected Airway Complication in a Male Patient with Goltz Syndrome
Case Reports in Anesthesiology, 2016 Goltz syndrome, also known as focal dermal hypoplasia, is a rare X-linked dominant multisystem syndrome presenting with cutaneous, skeletal, dental ocular, central nervous system and soft tissue abnormalities.
Sadie Smith +2 more
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Gorlin-Goltz syndrome: A rare case
Indian Journal of Dermatology, 2015 Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is characterized by multiple basocellular epitheliomas, keratocysts in the jaws, bifid ribs, palmar and/or plantar pits and ectopic calcifications of the falx cerebri.
Satyaki Ganguly +4 more
doaj +3 more sources
Multiple jaw cysts-unveiling the Gorlin-Goltz syndrome
Contemporary Clinical Dentistry, 2015 Gorlin-Goltz syndrome or basal cell nevus syndrome is a comparatively rare syndrome characterized by basal cell nevi, odontogenic keratocysts, and skeletal anomalies. Diagnosis is based on the major and minor clinical and radiographic criteria.
S Manjima +3 more
doaj +2 more sources
Goltz syndrome in male: A rare case of focal dermal hypoplasia
Indian Journal of Ophthalmology. Case Reports, 2023 Goltz syndrome or focal dermal hypoplasia is a rare meso-ectodermal, X-linked dominant genetic disorder with female preponderance. Though the involvement of multiple systems is present, the hallmark of this syndrome is typical cutaneous features.
Neha Kumari +3 more
doaj +2 more sources